Can Serum Lumican Level Identify a Hidden Fragility Phenotype Beyond Bone Mineral Density in Postmenopausal Women?

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age45+
SponsorKanuni Sultan Suleyman Training and Research Hospital

About this trial

Osteoporosis is a major cause of morbidity and fragility fractures in postmenopausal women. Bone mineral density (BMD) alone may not fully reflect fracture risk and skeletal fragility. Lumican, an extracellular matrix proteoglycan involved in collagen organization and musculoskeletal tissue homeostasis, has emerged as a potential biomarker for bone health. This prospective observational study aims to investigate the relationship between serum lumican levels, bone mineral density, muscle strength, and clinical fragility indicators in postmenopausal women. Approximately 100 participants will undergo routine osteoporosis assessment including DEXA, laboratory testing, FRAX evaluation, and handgrip strength measurement. The study will evaluate whether serum lumican levels can identify a hidden fragility phenotype beyond conventional bone mineral density measurements.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Female sex

Age 45 years or older

Postmenopausal status

Attendance at the Physical Medicine and Rehabilitation outpatient clinic

Disqualifiers

Premenopausal women

Secondary causes of osteoporosis (e.g., malignancy, advanced renal failure, severe liver disease, significant endocrine disorders)

Active infection or acute inflammatory disease

Major surgery within the previous 6 months

Trial population

The study population consists of postmenopausal women aged 45 years and older who attend the Physical Medicine and Rehabilitation outpatient clinic and undergo routine osteoporosis evaluation, including bone mineral density measurement by DEXA and standard osteoporosis laboratory testing. Participants will be recruited consecutively and enrolled after providing written informed consent.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

98 Participants
are grouped into 1 trial group
Group A: Postmenopausal Women Undergoing Osteoporosis Evaluation

Trial outcomes

Primary outcomes

1

Serum Lumican Level and Bone Mineral Density Association

Assessment of the relationship between serum lumican levels and bone mineral density (lumbar spine, total hip, and femoral neck BMD measured by DEXA).

Time frame
Baseline (at study enrollment)

Secondary outcomes

Other outcomes

Sponsors and contacts

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